System and method for correction of intracerebral chemical imbalances

ABSTRACT

A method of treating a central nervous system (CNS) disorder, comprises the steps of inserting into a patient&#39;s body first and second conduits so that distal ends of the first and second conduits open to a portion of the patient&#39;s CNS with direct access to cerebrospinal fluid (CSF) and a proximal end of the first conduit opens into a first reservoir of material to be introduced into the CSF and a proximal end of the second conduit opens to drain CSF withdrawn from the CNS in combination with the steps of detecting and analyzing brain activity of a patient and determining a chemical imbalance present in the CSF by one of a microassay of a sample of CSF withdrawn from the second reservoir and the detected and analyzed brain activity. Based on the determined chemical imbalance, the patient is treated by one of supplying an agent to the CSF via the first conduit and withdrawing a quantity CSF via the second conduit. A system for treating disorders of the central nervous system (CNS), comprises first and second conduits, wherein, when in an operative position, distal ends of the first and second conduits open into a portion of a patient&#39;s CNS with direct access to cerebrospinal fluid (CSF) and wherein, when in the operative position, a proximal end of the second conduit opens to drain CSF from the CNS and a first reservoir imlpantable within the patient&#39;s body and holding material to be introduced to the CNS in combination with a first pump coupled to the first reservoir and the first conduit for introducing the material to the CNS via the first conduit and a brain wave detection unit for detecting and analyzing brain waves of the patient.

BACKGROUND INFORMATION

The present invention relates generally to a system and method fortreating conditions of the brain. More specifically, the presentinvention relates to a catheter assembly and method for intraventricularshunting and lavage for the change of neurophysiological imbalances inthe central nervous system (CNS).

Apoprotein and other substances accumulate in the brain tissues ofpatients suffering from cognitive impairment associated with aging(e.g., Alzheimer's disease). Patients in a coma after traumatic headinjury, patients suffering from dementia, and patients with a variety ofother psychiatric disorders are also known to display imbalances ordeficiencies of a variety of cerebral neurotransmitters andelectrolytes.

Patients in a coma after traumatic head injury are known to displayseveral kinds of neurophysiological disequilibria, for example,excessively high intracranial pressure which may depress the regulationof vital functions or create deficits of neurotransmitters such asAcetylcholine or serotonin resulting in a diminution of activating andarousal processes.

Precursors and metabolites of neurotransmitters are also present in thecerebrospinal fluid (CSF) which establishes an equilibrium by diffusionwith the extracellular fluid (ECF) which is the intimate environment ofthe parenchyma tissue, neurons and glia. The CSF concentrations of thesesubstances may provide clinically useful information about excesses ordeficits of neurotransmitters in the tissue.

Such neurophysiological disequilibria may result in a build up of toxicsubstances in the CSF. Excessive amounts of metabolite produced in onebrain region may diffuse via the CSF to other regions where they mayalter the balance of reversible reactions. Intracranial pressure (ICP)may increase, causing depression of centers in the brainstem that areessential for maintenance and regulation of vital functions. Suchalterations of normal ICP are encountered in clinical conditions such ashydrocephalus or traumatic brain injury. The CSF may be drained from theCSF space to adjust the ICP, and the concentrations of metabolites orprecursors of critical substances may be subjected to microassay outsidethe cranium.

The removal of CSF to treat Alzheimer's disease, hydrocephalus, brainedema, or other diseases may be accomplished by the use of a variety ofintracranial devices, as is known in the art. To remove theseundesirable toxic substances or correct these undesirable pressures, adrainage device such as a shunt or a catheter may be placed in aventricle of the brain.

SUMMARY OF THE INVENTION

The present invention is directed to a method of treating a centralnervous system (CNS) disorder, comprising the steps of inserting into apatient's body first and second conduits so that distal ends of thefirst and second conduits open to a portion of the patient's CNS withdirect access to cerebrospinal fluid (CSF) and so that a proximal end ofthe first conduit opens into a first reservoir of material to beintroduced into the CSF and a proximal end of the second conduit opensto drain CSF withdrawn from the CNS and detecting and analyzing brainactivity of a patient in combination with the steps of determining achemical imbalance present in the CSF by one of a microassay of a sampleof CSF withdrawn from the second reservoir and the detected and analyzedbrain activity and treating the patient based on the determined chemicalimbalance by one of supplying an agent to the CSF via the first conduitand withdrawing a quantity CSF via the second conduit.

The present invention is further directed to a system for treatingdisorders of the central nervous system, comprising first and secondconduits, wherein, when in an operative position, distal ends of thefirst and second conduits open into a portion of a patient's CNS withdirect access to cerebrospinal fluid and wherein, when in the operativeposition, a proximal end of the second conduit opens to drain CSF fromthe CNS and at least one reservoir implantable within the patient's bodyand holding material to be introduced to the CNS in combination with afirst pump coupled to the first reservoir and the first conduit forintroducing the material to the CNS via the first conduit and a brainwave detection unit for detecting and analyzing brain waves of thepatient.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1A shows an exemplary embodiment of a catheter assembly accordingto the present invention;

FIG. 1B shows a cross-section of the catheter assembly of FIG. 1A takenalong line A-A of FIG. 1A;

FIG. 2A shows an exemplary embodiment of a first branch of the catheterassembly of FIG. 1A;

FIG. 2B shows a second branch of a catheter assembly according to anexemplary embodiment of the present invention;

FIG. 3 shows an osmotic pump assembly for use in accord with theembodiment of FIG. 1A;

FIG. 4 shows an exemplary embodiment of a method for the correction ofneurophysiological disequilibria in the central nervous system accordingto the present invention; and

FIG. 5 shows a cross-sectional view of a multi-chamber osmotic pumpaccording to an embodiment of the invention.

DETAILED DESCRIPTION

Those skilled in the art will understand that it may, at times, bedesirable to administer pharmacotherapeutic drugs or other therapeuticagents to treat chemical imbalances in the brain. However, the effectiveavailability of many of the pharmacotherapeutic drugs administered totreat such is limited by their inability to cross the blood-brainbarrier (“BBB”). Further, although precursors, agonists and antagonistsof these substances are well known, the ability to deliver effectivecerebral doses is sometimes seriously constrained by their possiblesystemic side effects.

Those skilled in the art will understand that it may, at times, bedesirable to adjust the ICP by removing CSF or by adding syntheticartificial CSF to optimize pressure dependent homeostatic functions.

The invention enables aggressive intervention in brain disorders byadaptively correcting the contribution of a suboptimal fluid environmentto the health of neural tissue, adjusting ICP or otherwise restoring anoptimal extracellular neurochemical balance by circumventing the brain'sresistance to drug entry posed by the BBB, as well as possible systemicside effects, by a direct delivery into the CSF using a minimallyinvasive technology coupled with bioassay and electrophysiologicalmonitoring techniques.

The CSF surrounding the brain and spine is naturally produced in thechorioid plexus in the ventricles and reabsorbed by arachnoid villi.Swelling of the brain due to edema caused by concussion commonly causesblockade of reabsorption pathways resulting in a pathological increasein ICP. Similar dangerous excesses of ICP and disturbances of braindevelopment can be caused by blockade of the cerebral ventricles inhydrocephalus. It is believed that certain brain disorders such as, forexample, Alzheimer's disease, may result from the presence of certaintoxic substances in the CSF. These toxins may, for example, be generatedby diseased neurons at a rate greater than the rate at which they areremoved by regeneration of the CSF, resulting in an accumulation oftoxins in the CSF. Known toxic substances include beta A-4 amyloid,beta-2 microglobulin, tau, etc. Other conditions are known to causeincreases or decreases in the availability of neurotransmitters or theirprecursors.

The ECF which is the intimate environment of the brain cells is inreversible diffusion exchange with the CSF and therefore conveysneurotransmitters and their precursors and metabolites from variousbrain regions into the CSF.

As would be understood by those skilled in the art, the power spectrumof the EEG is regulated by a homeostatic neuroanatomical system in thebrain which is dependent upon appropriate availability ofneurotransmitters. Excesses or deficits of these substances perturb thisregulation. Therefore, quantitative analysis of the EEG can serve as anindicator of neurotransmitter availability.

As would be understood by those skilled in the art, increases in ICPfollowing traumatic brain injury or other conditions may result inswelling of the brain and increases in the ICP that can have seriousconsequences including death, and are a subject of great concern in thetrauma intensive care unit.

The present invention is directed to a system and method for correctingsuch imbalances. In one embodiment of the invention, the system may beautomated to maintain a desired chemical balance in the CSF usingdynamic feedback from EEG monitoring and periodic chemical analysis ofthe CSF. However, a more basic system according to the present inventionmay include, for example, a shunting catheter for shunting CSF from thecranium and an infusion catheter for infusing necessary chemicals (i.e.,electrolytes, agonists, antagonists, etc.) into the cranium via anosmotic pump, while monitoring and regulating the effects of theintraventricular shunting and lavage with periodic quantitativeelectroencephalographic (QEEG) assays and with chemical analysis of theshunted CSF performed by clinical personnel.

In one embodiment of the invention, the system may be automated tomaintain a desired ICP using dynamic feedback from a sensor monitoringthe ICP to regulate the outflow of CSF from the shunt. For example, anindwelling pressure sensor may periodically detect ICP and forward thisdata to a processor so that, when an ICP value outside an acceptablerange is detected, external personnel may be notified or automaticcontrol of a pump to add or withdraw CSF may be undertaken until the ICPreturns to the acceptable range. Alternatively, as will be discussedbelow, brain activity may be monitored and the conclusions concerningthe level of ICP and actions to be taken may be made based on analysisof the brain activity detected. For example, data corresponding to theICP may be generated by evoking and analyzing brainstem auditoryresponses (BAER) as described in U.S. Pat. No. 4,705,049 (“the '049patent) the entire disclosure of which is hereby expressly incorporatedby reference herein.

FIGS. 1A and 1B show an exemplary embodiment of a catheter assembly 1according to the present invention. The catheter assembly 1 includes adual lumen catheter 100 and a data processing unit 200 which may includeeither or both of a QEEG monitor and a BAER monitor receiving data fromelectrodes placed on the scalp or under the skin as would be understoodby those skilled in the art. As would be understood, the components ofthe catheter assembly 1 may be made from any bio-compatible materials,such as, for example, silicon. As shown in FIG. 1B, a distal end of acatheter 100 which comprises a first lumen 110 and a second lumen 120 isinserted into a ventricle of a patient's brain as discussed in moredetail below. At some point along the length thereof, the first andsecond lumens 110, 120, respectively, of the catheter 100 divert intoseparate branches 110′ and 120′. Alternatively, as would be understoodby those of skill in the art, two single lumen catheters may besubstituted for the catheter 100 with a first one of the cathetersperforming the same functions as the first lumen 110, and a second oneof the catheters performing the same functions as the second lumen 120.As shown in FIG. 2A, the first lumen 110 extends past a valve 114 to areservoir 113 which is coupled to a pump 115 so that fluids and/ortherapeutic agents stored in the reservoir 113 may be fed through thefirst lumen to be supplied to the CSF. As shown in FIG. 2B, the proximalend of the branch 120′ is coupled via a valve 114′ to a receiving volume130 and a relief valve 116 controls drainage of the fluid within thereceiving volume 130 into the body. Exemplary internal locations for thereceiving volume 130 include the venous system, peritoneal cavity,pleural cavity, etc., and an exemplary external location may include adrainage bag. The valve 114 acts as a check valve to prevent a back-flowof CSF from the CNS into the pump 115 and the valve 114′ acts to preventthe flow of CSF into the receiving volume 130 to maintain a thresholdpressure in the cranium. The valves 114 and 114′ may, for example, beconstructed as described in U.S. Pat. No. 3,985,140 to Harris, which ishereby expressly incorporated by reference herein. Alternatively, thoseskilled in the art will recognize that the valves 114, 114′ may be anyother flow control component which controls the flow of CSF therethroughso that flow is prevented or allowed only in amounts and directions andat times desired by the system. As would be understood by those skilledin the art, the pump 115 may be an osmotic pump, micromechanical pump,or other conventional pump.

Alternatively, fluid may be drained into the patient's body. In thiscase, the second lumen 120 may include a plurality of small holes in thedistal end thereof, distal of the valve 114′, so that CSF accumulatingin the ventricle may enter the holes and drain from the catheter 100. Inaddition, a second pump (not shown) may be coupled to the second lumen120 to assist in drawing CSF from the CNS. The second lumen 120 allowsCSF to be withdrawn from the cranium, to remove accumulated, undesirabletoxic substances and/or to enable microassays of a withdrawn CSF sample.Furthermore, as would be understood by those skilled in the art, amicroassay or liquid chromatography chip or other suitable sensordifferentially sensitive to specific substances may automaticallyregularly or continuously sense concentrations of these specificsubstances (e.g., in the receiving volume 130) and compare theseconcentrations to optimal amounts. The results of these comparisons maythen be outputted to a clinician or may be sent directly to the dataprocessing unit 200, described in more detail below, to modify theoutput of the pump 115. The CSF may be extracted from the receivingvolume 130 for an external assay by puncturing the reservoir with aneedle and withdrawing the sample therefrom into a syringe. As would beunderstood by those skilled in the art, in such an arrangement theneedle would be inserted into a self-sealing septum so that, uponwithdrawal of the needle leakage from the receiving volume 130 would beprevented.

As mentioned above, a withdrawn CSF sample may be microassayed to makeadjustments and/or updates to balances of chemicals to be supplied tothe CSF (e.g., by altering the make-up of the fluid included in thereservoir 113). If, upon assay of the withdrawn CSF sample, the CSF isfound to contain undesirable material, it may be eliminated eitherspontaneously by withdrawing a quantity of the tainted CSF to spur thesecretion of new CSF by the brain, or forcibly by the introduction offluids via the first lumen 110 as described above. Furthermore, ifmicroassay of the withdrawn CSF sample reveals excess or deficientelectrolytes or the precursors or metabolites of cerebralneurotransmitters, the first lumen 110 may be used to infuseelectrolytes or agonists or antagonists of the deviant neurotransmitteror any other agent in order to restore a desired balance.

The removal of CSF, and thus, toxic substances contained therein via thesecond lumen 120 prevents these toxic substances from being reabsorbedand recirculated and makes it possible to manage levels of these toxins.In addition, since the removal rate of these toxins may be equal to, ifnot higher than, their production rates, newly produced, clean CSF willdisplace the contaminated fluid. Thus, a transport rate of the CSF maybe set at an optimum level to achieve and maintain a desired CSFcomposition. Those skilled in the art will understand that, CSFproduction varies significantly from patient to patient and,consequently, that the optimum transport levels will need to be variedas well to accommodate these differences.

In certain respects, the catheter 100 acts as a shunt system asdescribed, for example, in U.S. Pat. No. 3,654,932 to Newkirk, et al.,the disclosure of which is hereby incorporated by reference in itsentirety. The catheter assembly 1 is introduced into the ventricularsystem of the brain, preferably into the third ventricle, throughconventional surgery or any known technique as is done, for example, toregulate excess CSF in patients afflicted with hydrocephalus. Forexample, the catheter assembly 1 may be inserted through a burr hole ofthe skull and through the brain tissue, using a technique such as, forexample, the one described in U.S. Pat. No. 5,312,357 to Buijs et al.,the disclosure of which is hereby incorporated by reference in itsentirety. The proximal end of the first lumen 110 may be inserted, e.g.,into the patient's peritoneal cavity with the pump 115 and reservoir 113in a position such that the reservoir 113 may be easily accessed inorder to supply fluids and/or therapeutic agents thereto. As isgenerally done with ventricular shunts, the catheter assembly 1 mayultimately be covered and held in place by the scalp.

FIG. 3 shows in more detail an osmotic pump assembly (such as, forexample, described in U.S. Pat. No. 6,436,091 to Harper et al.) whichmay be employed as the osmotic pump 115 of FIG. 2A. The osmotic pumpassembly 115 comprises an osmotic reservoir 133 and an agent supplyreservoir 132. The osmotic pump assembly 115 supplies fluid from theagent supply reservoir 132 to the CNS via the valve 114 when aconcentration difference between the agent supply reservoir 132 and theosmotic reservoir 133 causes solvent to migrate across a semi-permeablemembrane 134 extending therebetween. The membrane 134 may be formed, forexample, of cellulose acetate or other suitable material as would beunderstood by those of skill in the art. As discussed in more detailbelow, the osmotic pump 115 may be replaced by a multi-chambered osmoticpump which can supply a combination of therapeutic agents to the CSF.

As would also be understood by those skilled in the art, the valves 114,114′ and/or the pump 115 may be activated to maintain a desired ICPbased on feedback from an indwelling pressure sensor. That is, the valve114′ may be operated to allow CSF to drain from the CNS when a detectedICP is above a predetermined threshold. Alternatively, the ICP data maybe output to allow manual adjustment of the ICP. Also, instead ofdirectly measuring the ICP, the data processing unit 200 may analyzebrain activity data and generate data corresponding to the ICP. Forexample, the data processing unit 200 may control a transmitting unit tosend out a trigger signal, collect BAER data, analyze a resultingwaveshape by optimal digital filtering and perform automatic peakdetection of the BAER waveshape. Then, an interval between first andfifth peaks of this waveshape is determined. If this interval is greaterthan a predetermined threshold length, it is determined that the ICP isnot optimum and, either this data is outputted to enable manual ICPadjustment or the data processing unit 200 controls the system to drainCSF until the BAER data indicates that the ICP is within the acceptablerange. For example, if the interval between the first and fifth peaks ofthe BAER waveshape is greater than 4.2 milliseconds, the systemdetermines that the level of the ICP is excessive (e.g., ICP>than 7.0Torre) and CSF may then be drained until the BAER data indicates thatthe ICP is <7.0 Torre (i.e., when the interval between the first andfifth peaks is equal to or less than 4.2 milliseconds). Of course, thoseskilled in the art will understand that BAER data may be combined withdetected pressure values if desired. In addition, a pump connected tothe second lumen 120 may be employed under control of the dataprocessing unit 200 to aid in draining CSF while the pump 115 may beused to add fluid to the CNS if the ICP is lower than a lower limit ofthe acceptable range.

In addition to the dual lumen catheter 100 and its components, asdescribed above the system data processing unit 200 may comprise a QEEGand/or BAER unit or other sensory evoked potential system, as shown inFIG. 1A. As would be understood by those skilled in the art, the dataprocessing unit 200 records and analyzes electrical activity of thebrain through the use of a high-speed data processor and electrodesplaced on or under the scalp and linked to the processor. The processorof the data processing unit 200 amplifies the detected electricalimpulses of the brain and converts them into a wave pattern to providebiofeedback corresponding to brain activity. Alternatively, other knownsystems for detecting and analyzing brain activity may be used tomonitor the same effects. The data processing unit 200 may be aconventional QEEG/BAER system utilizing electrodes removably attached toa patient's scalp and external data processing and monitoring equipment.Alternatively, the data processing unit 200 may be an implantable, fullyinternalized system directly linked to a central control unit whichgathers data from the data processing unit 200 and from other sourcesand controls components of the system such as the osmotic pump 131automatically to create a self regulating system. The electrodes for thedata processing unit 200 system may, for example, be implanted in amanner similar to that described for the implantation of brainstimulating electrodes in U.S. Pat. No. 6,463,328 the entire disclosureof which is hereby expressly incorporated by reference herein.

More specifically, the data processing unit 200 may comprise a QEEG unit200A, a BAER analyzer 200B and a transmitter 200C. The QEEG unit 200Apreferably operates as would be understood by those skilled in the artto perform all the functions of known quantitativeelectroencephalographic systems while the BAER analyzer 200B operates inconjunction with the transmitter 200C to analyze BAER data evoked byauditory stimulus generated by the transmitter. For example, thetransmitter 200C may send out a trigger signal, while the electrodesforward data to data processing unit 200. The BAER analyzer 200B theneliminates noise from the signal and analyzes the BAER waveshape byoptimal digital filtering and performs automatic peak detection of theBAER waveshape to determine the interval between the first and fifthpeaks. This data is then used by the data processing unit 200 to controlthe shunting of CSF to progressively adjust the ICP until the intervalbetween the first and fifth peaks of the BAER waveform is no greaterthan a predetermined threshold value (e.g., 4.2 milliseconds) or untilthe ICP is below a predetermined threshold (e.g., 7.0 Torre).

The data processing unit 200 may be used to monitor the effects of thechemicals and CSF interventions created by the present invention. It maygauge the rate and amount of infusion required by evaluating therestoration of any deviant brain electrical parameters to control datacorresponding to activity of the brain when symptoms of the CNS disorderare not present or to known normative values appropriate for the age,gender, etc. of the patient. Such age-appropriate normative data may,for example, be installed in a ROM unit of the data processing unit 200prior to implantation. Alternatively, the data processing unit 200 mayinclude an interface allowing for updated normative data to be providedthereto after implantation.

As described above, a plurality of electrodes coupled to the dataprocessing unit 200 are coupled to a patient's scalp. In addition, thedata processing unit 200 may be connected to the osmotic pump assembly115 so that operation of the pump 115 may be controlled thereby based onthe brain activity detected by the data processing unit 200. As would beunderstood by those of skill in the art, each of the plurality ofelectrodes is connected via a plurality of leads to the data processingunit 200 so that the data processing unit 200 acquires an EEG signal(i.e., brain-waves). The data processing unit 200 then analyzes andoperates on this EEG signal using, for example, spectral analysis. Theoutput from this EEG signal analysis is compared by the data processingunit 200 to reference data (e.g., normative values for the age of thepatient or data from taken from this patient when no symptoms (orreduced symptoms) of the CNS disorder were present). This analysis ismore fully described in the article John et al., “Neurometrics: ComputerAssisted Differential Diagnosis of Brain Dysfunctions” Science293:162-169, 1988 (“the Science Article”). The Science Article is herebyexpressly incorporated into this application in its entirety byreference. The analysis may indicate a deviation from the normsindicating that CSF should be drained or that therapeutic agents shouldbe infused. If so, the data processing unit 200 may provide a signal tothe osmotic pump assembly 115 or to the valve 114′ directing changesrequired to restore any deviant brain electrical parameters indicated bythe data analysis. For example, if the analysis indicates that aconcentration of a particular chemical being supplied to the CSF is at athreshold level or higher than desired, the data processing unit 200 maynotify the osmotic pump assembly 115 to reduce the rate of chemicalinfusion or stop it altogether until the detected brain activityindicates that the concentration of this chemical has dropped below thethreshold value. Or, if the analysis indicates an excessive level of atoxin produced within the brain, the data processing unit 200 may directthe forcible introduction of fluids to reduce the toxin concentration,etc. Of course, those skilled in the art will understand that in any orall of the cases, the data processing unit 200 may provide output datato an operator of the system who can override any automatic controlswhich the data processing unit 200 may be preparing to enact. Inaddition, the data processing unit 200 may alert the operator or thepatient whenever any of a plurality of predetermined conditions arises.

As described above, the data processing unit 200 is also connected tothe valve 114′ of the second lumen 120. After the EEG signal analysishas been conducted by the data processing unit 200 as described above,the data from the data processing unit 200 may be provided to anoperator who may make adjustments as necessary. Alternatively, the dataprocessing unit 200 directly control the valve 114′ based on this datato either increase or decrease an amount of CSF being drained from theventricle. Thus, the data processing unit 200 may regulate the drainageof CSF as well as the infusion of chemicals into the CSF.

FIG. 4 shows an exemplary embodiment of a method for the correction ofintracerebral chemical imbalances according to the present invention.Once the catheter assembly 1 has been inserted into the ventricle, CSFis drained through the second lumen 120 into the receiving volume 130(step 500) by opening the valve 114′. At the same time, the dataprocessing unit 200 then determines the ICP (step 510), microassays thefluid in the receiving volume 130 (step 520) and analyzes brain activity(step 530). Of course, those skilled in the art will understand that theremoval and/or assay of CSF via the second lumen 120 may be ongoingsimultaneously with the introduction of agents to the ventricle via thefirst lumen 110. Then, the ICP is compared to a predetermined threshold(step 540) and, if the ICP is greater than this amount, the valve 116 isopened to drain CSF from the CNS (step 550). If the ICP is less than thethreshold amount, the valve 116 is maintained closed (step 560). Basedon the analysis of brain activity in step 530 and the microassay of theCSF in step 520, the data processing unit 200 determines whether theinfusion of fluids or therapeutic agents is indicated (step 570). If theinfusion of fluids and/or therapeutic agents is indicated, the dataprocessing unit 200 determines the desired mix of fluids and/or agentsto be supplied (step 580). Then the data processing unit controls thepump 230 (described below) to supply the desired mix to the CNS (step590). Those skilled in the art will understand that the data processingunit 200 may analyze brain activity continuously or at regular intervalswith a delay factored in based on an expected time for the diffusion oftherapeutic agents to the targeted areas in the brain and that the datamay be interpreted by the data processing unit 200 as described, forexample, in the Science Article.

As shown in FIG. 5, a multi-chamber pump 230 which includes a pluralityof chemical reserves 232 may be substituted for the pump 115 of FIG. 1A.Each of the chemical reserves 232 is separated from a first solutereservoir 234 by a corresponding flexible membrane 236. The first solutereservoir 234 is separated from a second solute reservoir 238 by asemi-permeable membrane 240 and each of the chemical reserves isseparated from a mixing volume 233 in fluid communication with the firstlumen 10 by a corresponding valve 242. Thus, when a concentrationdifference exists between the first and second solute reservoirs 234,238, respectively, solvent migrates across the membrane 240 until theconcentrations on either side thereof are balanced. For example, if theconcentration of the solute is higher in the first solute reservoir 234than in the second solute reservoir 238, solvent moves across themembrane 240 from the second solute reservoir 238 into the first solutereservoir 234 to balance the concentrations. The increased volume ofsolvent in the first solute reservoir 234 exerts pressure on theflexible membrane 236. However, the flexible membranes 236 can not bemoved to expand this volume unless one or more of the valves 242 ismoved to the open position. A valve control mechanism 244 operates toopen a selected one or a selected plurality of the valves 242 so thatthe corresponding portion (or portions) of the flexible membrane 236 maybe pushed into the respective chemical reserve(s) 232 to supply thechemical(s) stored therein to the CSF via the mixing volume 233 and thefirst lumen 110. Alternatively, each chemical may be stored in aseparate chemical reserve and pumped from there into the CSF by acorresponding miniature piezo-electric or osmotic pump as would beunderstood by those skilled in the art.

Those skilled in the art will understand that the valve controlmechanism 244 may be coupled to the data processing unit 200 forautomatic control based on analysis of brain activity or, alternatively,may be controlled by an operator from outside the body using knownmagnetic switches, to achieve a desired balance of a plurality oftherapeutic agents supplied to the CSF. In addition a valve may beplaced between the mixing volume 233 and the first lumen 110 so thatselected chemicals may be mixed within the mixing volume 233 before theyare transported to the CSF via the first lumen 110.

There are many modifications of the present invention which will beapparent to those skilled in the art without departing form the teachingof the present invention. The embodiments disclosed herein are forillustrative purposes only and are not intended to describe the boundsof the present invention which is to be limited only by the scope of theclaims appended hereto.

1. A method of treating a central nervous system (CNS) disorder,comprising the steps of: inserting into a patient's body first andsecond conduits so that distal ends of the first and second conduitsopen to a portion of the patient's CNS with direct access tocerebrospinal fluid (CSF) and so that a proximal end of the firstconduit opens into a first reservoir of material to be introduced intothe CSF and a proximal end of the second conduit opens to drain CSFwithdrawn from the CNS; detecting and analyzing brain activity of apatient; determining a chemical imbalance present in the CSF by one of amicroassay of a sample of CSF and the detected and analyzed brainactivity; and treating the patient based on the determined chemicalimbalance by one of supplying an agent to the CSF via the first conduitand withdrawing a quantity of CSF via the second conduit.
 2. The methodaccording to claim 1, wherein the brain activity of the patient isdetected using one of a quantitative electroencephalography system and abrainstem auditory evoked response system analyzing brain activity ofthe patient, to identify brain activity corresponding to a predeterminedimbalance within the CSF.
 3. The method according to claim 1, whereinresults of the detection and analysis of the patient's brain activityare provided to treatment personnel who utilize the results to directthe treating of any detected chemical imbalance.
 4. The method accordingto claim 1, further comprising the step of providing a first pumpbetween the first reservoir and the distal end of the first conduit forcontrolling introduction of material from the first reservoir to theCSF.
 5. The method according to claim 4, wherein the first pump is anosmotic pump.
 6. The method according to claim 4, wherein the first pumpis a micro-mechanical pump.
 7. The method according to claim 4, whereinthe first reservoir includes a plurality of chambers with acorresponding therapeutic agent in each of the chambers and wherein thefirst pump draws from each of the chambers to supply a desired amount ofeach of the therapeutic agents to be supplied to the CSF.
 8. The methodaccording to claim 1, further comprising the step of providing pluralityof pumps between the first reservoir and the distal end of the firstconduit for controlling introduction of material from the firstreservoir to the CSF, wherein the first reservoir includes acorresponding plurality of chambers with a respective therapeutic agentin each of the chambers and wherein each of the pumps draws from thecorresponding chamber to supply a desired amount of each of therespective therapeutic agent to the CSF.
 9. The method according toclaim 1, wherein the proximal end of the second conduit opens into asecond reservoir into which the CSF is drained.
 10. The method accordingto claim 9, further comprising the step of providing a second pumpbetween the second reservoir and the distal end of the second conduitfor controlling withdrawal of CSF from the CNS.
 11. The method accordingto claim 10, wherein the second pump is an osmotic pump.
 12. The methodaccording to claim 10, wherein the second pump is a micro-mechanicalpump.
 13. The method according to claim 2, wherein the step of detectingand analyzing brain activity includes the substep of embedding the oneof a quantitative electroencephalography system and a brainstem auditoryevoked response system within a body of the patient.
 14. The methodaccording to claim 13, wherein the one of a quantitativeelectroencephalography system and a brainstem auditory evoked responsesystem provides output to treatment personnel who utilize the output todevise strategies for correcting the imbalance.
 15. The method accordingto claim 10, further comprising the steps of: embedding a one of aquantitative electroencephalography system and a brainstem auditoryevoked response system within the patient's body to detect and analyzebrain activity to identify brain activity corresponding to apredetermined imbalance within the CSF; and controlling the first andsecond pumps automatically based on output from the one of aquantitative electroencephalography system and a brainstem auditoryevoked response system to correct the imbalance.
 16. The methodaccording to claim 9, further comprising the step of withdrawing asample of fluid from the second reservoir for microassay by inserting asyringe into the second reservoir.
 17. The method according to claim 9,further comprising the step of detecting data corresponding to amicroassay of fluid within one of the second conduit and the secondreservior.
 18. The method according to claim 1, wherein the imbalance isa chemical imbalance in the CSF.
 19. The method according to claim 1,wherein the imbalance is an improper intracranial pressure.
 20. A systemfor treating disorders of the central nervous system (CNS), comprising:first and second conduits, wherein, when in an operative position,distal ends of the first and second conduits open into a portion of apatient's CNS with direct access to cerebrospinal fluid (CSF) andwherein, when in the operative position, a proximal end of the secondconduit opens to drain CSF from the CNS; a first reservoir implantablewithin the patient's body and holding a first material to be introducedto the CNS; a first pump coupled to the first reservoir and the firstconduit for introducing the first material to the CNS via the firstconduit; and a brain activity detection unit for detecting and analyzingbrain activity of the patient.
 21. The system according to claim 20,further comprising a second reservoir coupled to the proximal end of thesecond conduit for receiving CFS drained from the CNS.
 22. The systemaccording to claim 20, wherein the first pump is an osmotic pump. 23.The system according to claim 20, wherein the first pump is amicro-mechanical pump.
 24. The system according to claim 20, wherein thebrain activity detection unit of the patient is one of a quantitativeelectroencephalography system and a brainstem auditory evoked responsesystem analyzing brain activity of the patient, to identify brainactivity corresponding to a predetermined imbalance within the CSF. 25.The system according to claim 20, wherein the first reservoir includes aplurality of chambers with a corresponding therapeutic agent in each ofthe chambers and wherein the first pump draws from each of the chambersto supply a desired amount of each of the therapeutic agents to besupplied to the CSF.
 26. The system according to claim 25, wherein thefirst pump includes a plurality of pump units, each pump unit beingcoupled to a corresponding one of the chambers.
 27. The system accordingto claim 20, wherein the proximal end of the second conduit opens into asecond reservoir into which the CSF is drained.
 28. The system accordingto claim 27, further comprising a second pump between the secondreservoir and the distal end of the second conduit for controllingwithdrawal of CSF from the CNS.
 29. The system according to claim 28,wherein the second pump is an osmotic pump.
 30. The system according toclaim 28, wherein the second pump is a micromechanical pump.
 31. Thesystem according to claim 20, wherein the brain activity detection unitis embedded within a body of the patient.
 32. The system according toclaim 20, wherein the brain activity detection unit provides output totreatment personnel who utilize the output to devise strategies forcorrecting the imbalance.
 33. The system according to claim 20, whereinan output of the brain activity detection unit is coupled to the firstand second pumps to automatically control operation of the first andsecond pumps based on quantitative electroencephalography system outputto correct the imbalance.
 34. The system according to claim 33, whereinthe imbalance is a chemical imbalance in the CSF.
 35. The systemaccording to claim 33, wherein the imbalance is an improper intracranialpressure.
 36. An osmotic pump including: a plurality of agentreservoirs; first and second solute chambers; a semi-permeable membraneseparating the first and second solute chambers from one another; aflexible membrane separating a first one of the agent reservoirs fromthe first solute chamber; and a plurality of valves, each of the valvesmoveable between an open position in which a corresponding one of theagent reservoirs is open to an outlet of the pump and a closed positionin which the corresponding one of the agent reservoirs is sealed withrespect to the pump outlet.
 37. The osmotic pump according to claim 36,wherein the flexible membrane separates each of the agent reservoirsfrom the first solute chamber.
 38. The osmotic pump according to claim36, wherein the flexible membrane comprises a plurality of independentflexible members, each of the flexible members separating acorresponding one of the agent reservoirs from the first solute chamber.39. The osmotic pump according to claim 36, further comprising a valvecontrol mechanism for selectively moving each of the valves between itsopen and closed position.
 40. A system for treating disorders of thecentral nervous system (CNS), comprising: first and second conduits,wherein, when in an operative position, distal ends of the first andsecond conduits open into a portion of a patient's CNS with directaccess to cerebrospinal fluid (CSF) and wherein, when in the operativeposition, a proximal end of the second conduit opens to drain CSF fromthe CNS; a first reservoir implantable within the patient's body andholding a first material to be introduced to the CNS; intracranialpressure detecting unit; a first pump coupled to the first reservoir andthe first conduit for introducing the first material to the CNS via thefirst conduit; and a brain activity detection unit for detecting andanalyzing brain activity of the patient, the brain activity detectionunit controlling drainage of CSF based on input from the intracranialpressure detecting unit to maintain intracranial pressure within apredetermined range.
 41. The system according to claim 40, wherein theintracranial pressure detecting unit includes a pressure sensor.
 42. Thesystem according to claim 40, wherein the intracranial pressuredetecting unit analyzes electrical activity of the brain to determine acurrent intracranial pressure.
 43. The system according to claim 42,wherein the intracranial pressure detecting unit includes a transmitterfor providing auditory signals to the patient and a BAER analyzer foranalyzing brainstem evoked auditory potentials to determine a currentintracranial pressure.
 44. The system according to claim 40, wherein,when the intracranial pressure is greater than 7 Torre, the brainactivity detection unit drains CSF until the intracranial pressure is nogreater than 7 Torre.
 45. The system according to claim 43, wherein theBAER analyzer collects BAER data corresponding to auditory signalsgenerated by the transmitter and analyzes a BAER waveshape determinedbased on the BAER data to detect peaks of the BAER waveshape anddetermine a time interval between a first peak and a fifth peak of theBAER waveshape to determine the intracranial pressure.
 46. The systemaccording to claim 45, wherein, when the time interval between the firstand fifth peaks is greater than 4.2 milliseconds, the brain activitydetection unit determines that the intracranial pressure is excessiveand controls drainage of CSF to reduce the intracranial pressure.